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3,991 Possible Causes for Basal Cell Carcinoma, Posture Abnormal, Relative Macrocephaly in Childhood

  • Gorlin Syndrome

    […] syndrome (disorder) Naevoid basal cell carcinoma syndrome basal cell nevus syndrome Gorlin syndrome edit English nevoid basal cell carcinoma syndrome an autosomal dominant[wikidata.org] […] with NBCCS childhood medulloblastoma macrocephaly (occipital frontal circumference 97th centile) cleft lip/palate vertebral/rib anomalies preaxial or postaxial polydactyly[invitae.com] Hemivertebrae is a radiologic abnormality where the vertebrae of the patient is unable to develop properly thus resulting in problems with posture.[healthh.com]

  • Neurofibromatosis Type 1

    The number of café au lait macules increases with age in childhood, similar to what is observed in NF1 [Author, personal observation]. Macrocephaly.[web.archive.org] Gorlin Syndrome (nevoid basal cell carcinoma syndrome) Risk of developing cancerous and noncancerous tumors, most often basal cell carcinoma, less often meduloblastoma during[doi.org] Absolute or relative macrocephaly has been seen in children and adults with Legius syndrome.[web.archive.org]

  • Duchenne Muscular Dystrophy

    […] superfamily: AGM3, 6 Integrin: LAD1 Glanzmann's thrombasthenia Junctional epidermolysis bullosa with pyloric atresia EDAR (EDAR hypohidrotic ectodermal dysplasia) PTCH1 (Nevoid basal-cell[en.wikipedia.org] Camptocormia, or bent spine syndrome, is an abnormal posture consisting of forward flexion of the spine that disappears when a patient is supine.[ncbi.nlm.nih.gov] carcinoma syndrome) BMPR1A (BMPR1A juvenile polyposis syndrome) IL2RG (X-linked severe combined immunodeficiency) See also cell surface receptors v t e Diseases of collagen[en.wikipedia.org]

    Missing: Relative Macrocephaly in Childhood
  • Leigh's Disease

    , and rectum; basal cell carcinoma; leukemia; lymphoproliferative disorders such as Castleman syndrome; and Hodgkin lymphoma.[emedicine.medscape.com] Alexandra Wilson, the patient’s current attending physician, states that Emilio is unable to move his arms and legs and only has abnormal posturing movements with stimulation[lifeethics.org] A partial list includes non-SCLC; neuroendocrine carcinomas; lymphosarcoma; malignant thymoma; cancers of the breast, stomach, colon, prostate, bladder, kidney, gallbladder[emedicine.medscape.com]

    Missing: Relative Macrocephaly in Childhood
  • Fitzsimmons-Guilbert Syndrome

    CELL NEVUS SYNDROME NEVOID BASAL CELL CARCINOMA (BCC) SYNDROME GORLIN-GOLTZ SYNDROME syndrome of autosomal dominant inheritance characterized by (1) multiple cutaneous basal[radiologykey.com] Relative macrocephaly is present during early childhood but head circumference is markedly low by adulthood. Psychomotor development is normal.[nectarmutation.org] Characteristic radiographic findings of thickening of the calvarium, sclerotic epiphyses, vertebral and pelvic abnormalities Infants: 2 Major alone is sufficient for diagnosis[entokey.com]

  • Tuberculosis

    The “eczema” was found to be a basal cell carcinoma, which was swiftly removed.[theguardian.com]

    Missing: Relative Macrocephaly in Childhood
  • Sotos Syndrome

    […] of life, and/or basal cell carcinomas usually from the third decade onwards.[ncbi.nlm.nih.gov] She has basal cell and squamous cell carcinoma for which her lifetime of sun exposure and fair cutaneous phototype are viewed as risk factors.[ncbi.nlm.nih.gov] Nevoid basal cell carcinoma syndrome (NBCCS, or Gorlin syndrome) is characterized by the development of multiple jaw keratocysts, frequently beginning in the second decade[ncbi.nlm.nih.gov]

    Missing: Relative Macrocephaly in Childhood
  • Phakomatosis Pigmentokeratotica

    Pagina 369 - Nevoid basal cell carcinoma syndrome in a person with dark skin. J Am Acad Dermatol 2003; 49: 332-5 LeSueur BW, Silvis NG, Hansen RC.[books.google.ro] There were no abnormalities with the upright position and movement coordination.[doi.org] Cell Carcinomas. ( 28937433 ) Loh S.H....Sim W.Y. 2017 4 HRAS mutation in phacomatosis pigmentokeratotica without extracutaneous disease. ( 28736904 ) Jennings L....O'Kane[malacards.org]

    Missing: Relative Macrocephaly in Childhood
  • Becker Nevus Syndrome

    cell carcinomas represent nevoid basal cell carcinoma syndrome. 6 Rahbari and Mehregan 7 noted that 2% of patients younger than 45 years of age with basal cell carcinomas[nature.com] There were no abnormalities with the upright position and movement coordination.[jamanetwork.com] Seite 369 - Nevoid basal cell carcinoma syndrome in a person with dark skin. J Am Acad Dermatol 2003; 49: 332-5 LeSueur BW, Silvis NG, Hansen RC.[books.google.de]

    Missing: Relative Macrocephaly in Childhood
  • Prader-Willi Syndrome

    […] superfamily: AGM3, 6 Integrin: LAD1 Glanzmann's thrombasthenia Junctional epidermolysis bullosa with pyloric atresia EDAR (EDAR hypohidrotic ectodermal dysplasia) PTCH1 (Nevoid basal-cell[en.wikipedia.org] carcinoma syndrome) BMPR1A (BMPR1A juvenile polyposis syndrome) IL2RG (X-linked severe combined immunodeficiency) See also cell surface receptors v t e Diseases of collagen[en.wikipedia.org]

    Missing: Relative Macrocephaly in Childhood